FDA 510(k) Application Details - K022540

Device Classification Name	Recorder, Magnetic Tape, Medical   More FDA Info for this Device
510(K) Number	K022540
Device Name	Recorder, Magnetic Tape, Medical
Applicant	ROZINN ELECTRONICS, INC. 71-22 MYRTLE AVE. GLENDALE, NY 11385 US Other 510(k) Applications for this Company
Contact	MARK ROSOFF Other 510(k) Applications for this Contact
Regulation Number	870.2800   More FDA Info for this Regulation Number
Classification Product Code	DSH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/01/2002
Decision Date	10/24/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review